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Prevention of Stroke in Women

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Cerebral Venous Thrombosis (CVT) Î In patients with suspected CVT, routine blood studies consisting of a complete blood count, chemistry panel, prothrombin time, and activated partial thromboplastin time should be performed (I-C). Î Screening for potential prothrombotic conditions that may predispose a person to CVT (eg, use of contraceptives, underlying inflammatory disease, infectious process) is recommended in the initial clinical assessment (I-C). Î Testing for prothrombotic conditions, including protein C, protein S, or antithrombin deficiency; antiphospholipid syndrome; prothrombin G20210A mutation; and factor V Leiden can be beneficial for the management of patients with CVT. Testing for protein C, protein S, and antithrombin deficiency is generally indicated 2-4 weeks after completion of anticoagulation. There is a very limited value of testing in the acute setting or in patients taking warfarin (IIa-B). Î In patients with provoked CVT (associated with a transient risk factor), vitamin K antagonists with a target INR of 2.0-3.0 may be continued for 3-6 months (IIb-C). Î In patients with unprovoked CVT, vitamin K antagonists may be continued for 6-12 months, with a target INR of 2.0-3.0 (IIb-C). Î For patients with recurrent CVT, VTE after CVT, or first CVT with severe thrombophilia (ie, homozygous prothrombin G20210A; homozygous factor V Leiden; deficiencies of protein C, protein S, or antithrombin; combined thrombophilia defects; or antiphospholipid syndrome), indefinite anticoagulation with a target INR of 2.0-3.0 may be considered (IIb-C). Î For women with CVT during pregnancy, LMWH in full anticoagulant doses should be continued throughout pregnancy, and LMWH or vitamin K antagonist with a target INR of 2.0-3.0 should be continued for ≥6 weeks postpartum (for a total minimum duration of therapy of 6 months) (I-C). Î It is reasonable to advise women with a history of CVT that future pregnancy is not contraindicated. Further investigations regarding the underlying cause and a formal consultation with a hematologist or maternal-fetal medicine specialist are reasonable (IIa-B). Î It is reasonable to treat acute CVT during pregnancy with full-dose LMWH rather than unfractionated heparin (IIa-C). Î For women with a history of CVT, prophylaxis with LMWH during future pregnancies and the postpartum period is reasonable (IIa-C).

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